Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

BACKGROUND: Osteochondroma generally occurs as a single lesion and it is not a heritable disease. When two or more osteochondroma are present, this condition represents a genetic disorder named hereditary multiple exostoses (HME). Growth hormone deficiency (GHD) has rarely been found in HME patients...

Descripción completa

Detalles Bibliográficos
Autores principales: Bozzola, Mauro, Gertosio, Chiara, Gnoli, Maria, Baronio, Federico, Pedrini, Elena, Meazza, Cristina, Sangiorgi, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524199/
https://www.ncbi.nlm.nih.gov/pubmed/26239617
http://dx.doi.org/10.1186/s13052-015-0162-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524199/
https://www.ncbi.nlm.nih.gov/pubmed/26239617
http://dx.doi.org/10.1186/s13052-015-0162-2

Ejemplares similares